§1.95. Application for authorization to relabel and recondition.
21 C.F.R. § 1.95
Application for authorization to relabel or perform other action to bring the article into compliance with the Federal Food, Drug, and Cosmetic Act or to render it other than a food, drug, device, or cosmetic may be filed only by the owner or consignee, and shall:
Contain detailed proposals for bringing the article into compliance with the act or rendering it other than a food, drug, device, or cosmetic.
Specify the time and place where such operations will be carried out and the approximate time for their completion.
Notes, amendments, and revision history
Amendments
[42 FR 15553, Mar. 22, 1977, as amended at 85 FR 50781, Aug. 18, 2020]
Authority
Authority: 15 U.S.C. 1333, 1453, 1454, 1455, 4402; 19 U.S.C. 1490, 1491; 21 U.S.C. 321, 331, 332, 333, 334, 335a, 342, 343, 350c, 350d, 350j, 352, 355, 360b, 360ccc, 360ccc-1, 360ccc-2, 362, 371, 374, 381, 382, 384a, 387, 387a, 387c, 393, and 2223; 42 U.S.C. 216, 241, 243, 262, 264, 271.
Source
Source: 42 FR 15553, Mar. 22, 1977, unless otherwise noted.
Amendments
[42 FR 15553, Mar. 22, 1977, as amended at 85 FR 50781, Aug. 18, 2020]